A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838987



Internal ID22613922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:31461843..31467942hg38UCSC Ensembl
chr4:31463465..31469564hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg386100
hg196100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1566n209
Supporting Variantsnssv17493488
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838987
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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